Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.23 (C)
Location

Chromosome 3:16586299 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58146551

HGVS name

3:g.16586299A>C

This variation has assays on 12 chips - click the plus to show

Variation displays